✦ LIBER ✦
Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome
✍ Scribed by S. Voutoufianakis; S. Psoni; P. Vorgia; F. Tsekoura; K. Kekou; J. Traeger-Synodinos; S. Kitsiou; E. Kanavakis; H. Fryssira
- Book ID
- 113590182
- Publisher
- Elsevier Science
- Year
- 2007
- Tongue
- English
- Weight
- 518 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1090-3798
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